An Enzyme‐Engineered Coppery Nanozyme for High‐Efficiency Mild Photothermal/Chemodynamic/Starvation Therapy Through Self‐Reinforcing Cancer Energy Metabolism Regulation

Author:

Bian Yulong12,Liu Bin13,Ding Binbin1,Yuan Meng12,Yang Chunzheng12,Li Kai1,Chang Mengyu4,Kheraif Abdulaziz A. Al5,Ma Ping'an12ORCID,Lin Jun12

Affiliation:

1. State Key Laboratory of Rare Earth Resource Utilization Changchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun 130022 China

2. School of Applied Chemistry and Engineering University of Science and Technology of China Hefei 230026 China

3. Key Laboratory of Superlight Materials and Surface Technology Ministry of Education College of Materials Science and Chemical Engineering Harbin Engineering University Harbin 150001 China

4. Departments of Radiation Oncology The University of Texas MD Anderson Cancer Center Houston TX 77030 USA

5. Dental Health Department College of Applied Medical Sciences King Saud University Riyadh 12372 Saudi Arabia

Abstract

AbstractPhotothermal therapy (PTT) has a great prospect in further improving tumor therapeutic outcomes, whereas its efficiency is restrained by low light penetration, excessive heat damage to normal tissues, up‐regulated heat shock proteins (HSPs), and limited effect of single treatment. Herein, an enzyme‐engineered coppery nanozyme based on dendritic mesoporous coppery carbon nanosphere as the cornerstone to load with glucose oxidase (GOx) followed by modification with hyaluronic acid is constructed. Density functional theory calculations indicate that the obtained coppery nanozyme exhibits peroxidase and glutathione oxidase mimicking activities to improve hydroxyl radicals (•OH) production. Furthermore, both the generation of •OH production and GOx‐induced energy supply blockade can reduce HSPs expression to enhance the mild PTT (η = 34.9 %) of coppery nanozyme upon the irradiation of 1064 nm laser, and in turn, accelerate the catalytic processes of coppery nanozyme for more generation of •OH. Last but not least, the introduction of copper can induce lipoylated protein dihydrolipoamide S‐acetyltransferase aggregation to cause cellular cuproptosis. Due to the synergy of multiple therapies, the tumor inhibition rate can reach 93.4%. Overall, this work provides an effective strategy for potential tumor treatment on the basis of synergistic therapies.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Publisher

Wiley

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